Citalopram for Agitation in Alzheimer's Disease
NCT00898807 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 186
Last updated 2014-06-27
Summary
The purpose of this study is to evaluate the safety and efficacy of citalopram for agitation in Alzheimer's dementia.
Conditions
- Alzheimer's Disease
- Agitation
Interventions
- DRUG
-
citalopram
target dose 30mg daily for 9 weeks
- DRUG
-
daily for 9 weeks
Sponsors & Collaborators
-
National Institute on Aging (NIA)
collaborator NIH -
National Institute of Mental Health (NIMH)
collaborator NIH -
JHSPH Center for Clinical Trials
lead OTHER
Principal Investigators
-
Constantine Lyketsos, MD, MHS · Johns Hopkins University
-
Lon Schneider, MD · University of Southern California Keck School of Medicine Memory and Aging Center
-
Bruce Pollock, MD · Centre for Addiction and Mental Health
-
Jacobo Mintzer, MD · Medical University of South Carolina Alzheimer's Research and Clinical Programs
-
David Shade, Esq · Johns Hopkins University
-
Davengere Devanand, MD · Columbia University
-
Paul Rosenberg, MD · Johns Hopkins University
-
Daniel Weintraub, MD · University of Pennsylvania
-
Anton Porsteinsson, MD · University of Rochester
-
Jerome Yesavage, MD · Stanford University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-07-31
- Primary Completion
- 2013-09-30
- Completion
- 2013-09-30
Countries
- United States
- Canada
Study Locations
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